Test Price
2,800 AED✅ Home Collection Available
F2 (Prothrombin) Gene Mutation Analysis (NGS) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل طفرة جين البروثرومبين (F2) لعوز العامل الثاني عبر التسلسل الجيني NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Patient Trust Commitment
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
دقة تشخيصية 99.9%، خدمة سحب منزلي معتمدة، إرشاد سريري بعد التحليل. الامتثال للمرسوم بقانون اتحادي رقم 41 لسنة 2024 (المادة 87) وقانون حماية البيانات الشخصية الإماراتي.
Overview
The F2 (Prothrombin) Gene Mutation Analysis via Next-Generation Sequencing (NGS) identifies the G20210A variant associated with inherited thrombophilia, aiding in risk stratification for venous thromboembolism. (يوفر تحليل طفرة جين البروثرومبين تقييماً دقيقاً للاستعداد الوراثي للتخثر الوريدي).
| Feature | Our Test (NGS) | Closest Alternative (PCR) |
|---|---|---|
| Precision | Single‑nucleotide resolution, full gene coverage | Targeted mutation detection, limited to known hotspot |
| Method | Next‑Generation Sequencing (LC‑MS/MS validated) | Allele‑specific PCR |
| Speed | 3–4 Weeks (comprehensive analysis) | 1–2 Weeks |
Physician Insight & Safety Protocol
“I understand that genetic testing can be daunting. This test helps identify inherited thrombophilia risk but must be interpreted alongside your personal and family history. Please always consult your haematologist for a comprehensive evaluation.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Safety Exclusion Criteria & Emergency Red Flags
- This test is not a stand‑alone diagnostic tool; genetic counselling is mandatory before sampling.
- Exclusion: Cannot be performed on patients with recent allogeneic bone marrow transplant (potential donor DNA interference).
- Emergency Red Flags: Sudden severe leg pain, unexplained chest pain, shortness of breath, or one‑sided limb swelling may indicate acute thrombosis. Seek immediate emergency care.
Patient FAQ & Clinical Guidance
1. What does a positive F2 prothrombin mutation result actually mean for my health?
A positive result indicates you carry one copy of the G20210A mutation, which increases your lifetime risk of venous thromboembolism by 3‑ to 5‑fold compared to the general population, but does not guarantee a clot will form. وجود الطفرة لا يعني حتمية حدوث جلطة، بل يتطلب إدارة طبية وقائية تحت إشراف أخصائي أمراض الدم.
2. How is the sample collected and what is the process?
A trained phlebotomist collects a simple blood sample (or one drop of blood on an FTA card) during your home visit; extracted DNA is then analysed with NGS in our ISO‑certified laboratory. تتوفر خدمة السحب المنزلي المعقمة والمعتمدة، ولا تحتاج لتحضيرات خاصة قبل الفحص.
3. When will I receive my results and how will they be explained?
Final report with clinical interpretation is delivered within 3 to 4 weeks; a free telephonic post‑ session with a clinical genetic counsellor is included to explain every detail. يشمل السعر جلسة إرشاد وراثي عن بُعد لضمان فهمك الكامل للنتائج وتوجيهك للخطة الوقائية.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians